3554-91-4

Benzyl 2-acetamido-2-deoxy-4,6-O-benzylidene-α-D-galactopyranoside Chemical Structure
3554-91-4

Chemical Structure

Benzyl 2-acetamido-2-deoxy-4,6-O-benzylidene-α-D-galactopyranoside

  • CAS No.: 3554-91-4
  • Formula:C22H25NO6
  • Molecular Weight:399.44

IUPAC Name: N-((4aR,6S,7R,8R,8aR)-6-(benzyloxy)-8-hydroxy-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-yl)acetamide

InChIKey: NXGXFAKJUWEFEC-JPMMBXSKSA-N

SMILES: O[C@@H]1[C@H]([C@H](O[C@@H]2COC(O[C@@H]21)C3=CC=CC=C3)OCC4=CC=CC=C4)NC(C)=O

Biological Activity: Benzyl 2-acetamido-2-deoxy-4,6-O-benzylidene-α-D-galactopyranoside is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology[1].

Cat. No. Product Name Purity Description Pricing
HY-W699293
Benzyl 2-acetamido-2-deoxy-4,6-O-benzylidene-α-D-galactopyranoside Benzyl 2-acetamido-2-deoxy-4,6-O-benzylidene-α-D-galactopyranoside is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology.
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